A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491997



Internal ID21149550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:59997001..59998900hg38UCSC Ensembl
chr14:60463719..60465618hg19UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18020461
Samples
Known GenesLRRC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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